Just bought my first cane

[aryannevt]

So it's been a year since I first started on this journey. Now I'm walking it with the help of a cane. While I'm still not diagnosed it seems I'm getting closer. I realize there are much worse things than MS but there are days when this is a bit hard to take!!

[karryon55]

I've been using Canes since I was in my 20's & I just try to not think of the stigma of it being something a granny would use lol. They are always handing if someone tries to steel your purse and great for those annoying relatives that may give you any cheek. :D

On the serious side though I have moved from canes to crutches to 4 wheel walkers to wheelchair to scooter and back again that I just choose the appropriate aid for the day. I think I've been using aids too long to worry what others think anymore and this happens to everyone.

You can decorate them elaborately or keep them plain but always have your details somewhere on it incase you leave it somewhere.

Take Care,

Karry.

[Lulu54]

I keep the canes handy - yes, a couple different types including a folding one that I can travel with.  I think of it as having a third leg to help me walk when I need the extra assistance with balance.  It does make a huge difference.

Good luck with the diagnosis - it can take years for some people when the symptoms or evidence are not obvious.   - Laura

[aryannevt]

Thanks for the kind word and support!! It was a no brainier. Tired of being stuck on bleachers waiting for an arm to hold on to : ) and not willing to give up watching my kids play sports. It's pretty freeing really....caring less about what other people think and more about what works for me and mine.

[davincidanes]

I can relate, but certainly not quite there yet.  In November my husband asked me what I wanted for Christmas and I jokingly (but not really), said "a cane".  However, shortly after I had my first round of IVSM that greatly improved my mobility. - So issue averted for the time being.  I hope you do well with it.

~Linda

[4happygnomes]

I promise I didn't swear...the word I used that were starred out by the site rhymes with "ducks"...;-)

[4happygnomes]

I'm also still in limbo and unfortunately, the greatest impact of what ever "this" is, is effecting my ability to walk correctly/smoothly.  I just wanted to say that I admire your courage.  I'm afraid I too might have to rely on a cane, and I'm having a hard time coming to terms with that...and not quite brave enough to take that next step.  I agree, this situation *****!

It takes strength to show our weakness...stay strong!  

Karen

[HVAC]

I know it is hard. I have known people with MS who had to use a cane for awhile and then they got better and did not need it. I hope you found one you like. There are so many choices of colors and all now days.

Alex